Canonical Allele Identifier: CA755278187

Gene: IL1RN

Linked Data

• dbSNP Id: rs1395400714
• gnomAD v3: 2-113133279-C-CA
• gnomAD v4: 2-113133279-C-CA
• MyVariant Identifiers: chr2:g.113890856_113890857insA (hg19) ; chr2:g.113133279_113133280insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113133285dup , CM000664.2:g.113133285dup	GRCh38
NC_000002.11:g.113890862dup , CM000664.1:g.113890862dup	GRCh37
NC_000002.10:g.113607333dup	NCBI36
NG_021240.1:g.20393dup , LRG_188:g.20393dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.*414dup	ENSP00000387210.1:n.*414dup
ENST00000696879.1:c.*414dup	ENSP00000512947.1:n.*414dup
ENST00000696880.1:c.*212-80dup	ENSP00000512948.1:n.*212-80dup
ENST00000696882.1:c.*718dup	ENSP00000512950.1:n.*718dup
ENST00000409930.4:c.*414dup MANE Select	ENSP00000387173.3:n.*414dup
ENST00000259206.9:c.*414dup	ENSP00000259206.5:n.*414dup
ENST00000354115.6:c.*414dup	ENSP00000329072.3:n.*414dup
ENST00000361779.7:c.*414dup	ENSP00000354816.3:n.*414dup
ENST00000409052.5:c.*414dup	ENSP00000387210.1:n.*414dup
NM_000577.4:c.*414dup	NP_000568.1:n.*414dup
NM_173841.2:c.*414dup , LRG_188t1:c.*414dup	NP_776213.1:n.*414dup
NM_173842.2:c.*414dup	NP_776214.1:n.*414dup
NM_173843.2:c.*414dup	NP_776215.1:n.*414dup
XM_005263661.3:c.*414dup	XP_005263718.1:n.*414dup
XM_006712497.2:c.*414dup	XP_006712560.1:n.*414dup
XM_011511121.1:c.*414dup	XP_011509423.1:n.*414dup
NM_001318914.1:c.*414dup	NP_001305843.1:n.*414dup
XM_005263661.4:c.*414dup	XP_005263718.1:n.*414dup
NM_000577.5:c.*414dup	NP_000568.1:n.*414dup
NM_001318914.2:c.*414dup	NP_001305843.1:n.*414dup
NM_173842.3:c.*414dup MANE Select	NP_776214.1:n.*414dup
NM_173843.3:c.*414dup	NP_776215.1:n.*414dup
NM_001379360.1:c.*414dup	NP_001366289.1:n.*414dup
NM_173841.3:c.*414dup	NP_776213.1:n.*414dup